Prenatal and postnatal prevalence of Turner's syndrome

BMJ

Volumn 313, Issue 7048, 1996, Pages 47-

  Van Der Sijs Bos, C J M ^a   Stigter, R H ^b   Christiaens, G C M L ^c   Leschot, N J ^d  

^a Dutch Working Party on Prenatal Diagnosis ^*  (Netherlands)

^b Clinical geneticist Clinical Genetic Centre   (Netherlands)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^d UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; CHORION VILLUS SAMPLING; CHROMOSOME MOSAICISM; CYTOGENETICS; HUMAN; KARYOTYPE; LETTER; PERINATAL PERIOD; PRENATAL SCREENING; PREVALENCE; PRIORITY JOURNAL; TURNER SYNDROME;

DIAGNOSTIC ERRORS; FEMALE; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS; PREVALENCE; TURNER SYNDROME;

EID: 0030003368     PISSN: 09598138     EISSN: 14685833     Source Type: Journal    
DOI: 10.1136/bmj.313.7048.47b     Document Type: Letter

References (3)

1. Gravholt CH, Juul S, Naeraa RW, Hansen H. Prenatal and postnatal prevalence of Turner's syndrome: a registry study. BMJ 1996; 312: 16–21. (6 January.)
2. Davee MA, Weaver WD. Turner syndrome.In: Buyse ML., ed.Birth defects encyclopedia. Oxford: Blackwell, 1990: 1717–9.
3. Leschot NJ, Wolf H, Verjaal M, van Prooijen-Knegt AC, Boer B. Monosomy X found at first trimester CVS: a diagnostic and counselling dilemma. Clin Genet 1990; 37: 236–237.